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NCT01292759 Clinical Trial

Non-invasive Assessment of Arterial Blood Pressure and Functional Hemodynamic Parameters

Surgical Procedure, Unspecified Clinical Trial

Official title:
An Evaluation of a New, Non-invasive Monitoring Device in Major Abdominal Surgery Patients

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT01292759
Other study ID # 837.194.10 (7203)
Secondary ID
Status Recruiting
Phase N/A
First received February 9, 2011
Last updated February 14, 2011
Start date July 2010

Study information
Verified date July 2010
Source Johannes Gutenberg University Mainz
Contact n/a
Is FDA regulated No
Health authority Germany: Ethics Commission
Study type Observational

Clinical Trial Summary

Cardiac output can be monitored using different invasive devices. Nexfin HD is a new, noninvasive device that uses model flow technology to measure stroke volume and thus computes cardiac output (CO). To evaluate this new device the investigators compared esophageal doppler CO to Nexfin HD CO in patients scheduled for elective abdominal surgery.

Recruitment information / eligibility
Status Recruiting
Enrollment 24
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Age > 18 and < 80 years old

- Written informed consent obtained

Exclusion Criteria:

- Renal failure

- Heart failure (EF < 25%)

- Peripheral artery occlusion disease

- M. Raynaud

- Rhythms other than sinus

Study Design

Observational Model: Case-Only, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Germany Klinik für Anaesthesiology der Universitätsmedizin Mainz Mainz

Sponsors (1)
Lead Sponsor Collaborator
Johannes Gutenberg University Mainz

Country where clinical trial is conducted

Germany, 

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